739 related articles for article (PubMed ID: 11106718)
1. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
Kamisago M; Sharma SD; DePalma SR; Solomon S; Sharma P; McDonough B; Smoot L; Mullen MP; Woolf PK; Wigle ED; Seidman JG; Seidman CE
N Engl J Med; 2000 Dec; 343(23):1688-96. PubMed ID: 11106718
[TBL] [Abstract][Full Text] [Related]
2. Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly.
Niimura H; Patton KK; McKenna WJ; Soults J; Maron BJ; Seidman JG; Seidman CE
Circulation; 2002 Jan; 105(4):446-51. PubMed ID: 11815426
[TBL] [Abstract][Full Text] [Related]
3. [Mutations in genes for sarcomeric proteins].
Kimura A
Nihon Rinsho; 2000 Jan; 58(1):117-22. PubMed ID: 10885298
[TBL] [Abstract][Full Text] [Related]
4. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.
Kaski JP; Syrris P; Burch M; Tomé-Esteban MT; Fenton M; Christiansen M; Andersen PS; Sebire N; Ashworth M; Deanfield JE; McKenna WJ; Elliott PM
Heart; 2008 Nov; 94(11):1478-84. PubMed ID: 18467357
[TBL] [Abstract][Full Text] [Related]
5. Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
Kärkkäinen S; Heliö T; Jääskeläinen P; Miettinen R; Tuomainen P; Ylitalo K; Kaartinen M; Reissell E; Toivonen L; Nieminen MS; Kuusisto J; Laakso M; Peuhkurinen K
Eur J Heart Fail; 2004 Dec; 6(7):861-8. PubMed ID: 15556047
[TBL] [Abstract][Full Text] [Related]
6. Mutations in sarcomere protein genes in left ventricular noncompaction.
Klaassen S; Probst S; Oechslin E; Gerull B; Krings G; Schuler P; Greutmann M; Hürlimann D; Yegitbasi M; Pons L; Gramlich M; Drenckhahn JD; Heuser A; Berger F; Jenni R; Thierfelder L
Circulation; 2008 Jun; 117(22):2893-901. PubMed ID: 18506004
[TBL] [Abstract][Full Text] [Related]
7. Advances in the Genetic Basis and Pathogenesis of Sarcomere Cardiomyopathies.
Yotti R; Seidman CE; Seidman JG
Annu Rev Genomics Hum Genet; 2019 Aug; 20():129-153. PubMed ID: 30978303
[TBL] [Abstract][Full Text] [Related]
8. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
[TBL] [Abstract][Full Text] [Related]
9. Sarcomeric protein mutations in dilated cardiomyopathy.
Chang AN; Potter JD
Heart Fail Rev; 2005 Sep; 10(3):225-35. PubMed ID: 16416045
[TBL] [Abstract][Full Text] [Related]
10. Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.
Lakdawala NK; Dellefave L; Redwood CS; Sparks E; Cirino AL; Depalma S; Colan SD; Funke B; Zimmerman RS; Robinson P; Watkins H; Seidman CE; Seidman JG; McNally EM; Ho CY
J Am Coll Cardiol; 2010 Jan; 55(4):320-9. PubMed ID: 20117437
[TBL] [Abstract][Full Text] [Related]
11. Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
Dellefave LM; Pytel P; Mewborn S; Mora B; Guris DL; Fedson S; Waggoner D; Moskowitz I; McNally EM
Circ Cardiovasc Genet; 2009 Oct; 2(5):442-9. PubMed ID: 20031619
[TBL] [Abstract][Full Text] [Related]
12. Lifelong Clinical Impact of the Presence of Sarcomere Gene Mutation in Japanese Patients With Hypertrophic Cardiomyopathy.
Nakashima Y; Kubo T; Sugiura K; Ochi Y; Takahashi A; Baba Y; Hirota T; Yamasaki N; Kimura A; Doi YL; Kitaoka H
Circ J; 2020 Sep; 84(10):1846-1853. PubMed ID: 32830170
[TBL] [Abstract][Full Text] [Related]
13. Perturbed length-dependent activation in human hypertrophic cardiomyopathy with missense sarcomeric gene mutations.
Sequeira V; Wijnker PJ; Nijenkamp LL; Kuster DW; Najafi A; Witjas-Paalberends ER; Regan JA; Boontje N; Ten Cate FJ; Germans T; Carrier L; Sadayappan S; van Slegtenhorst MA; Zaremba R; Foster DB; Murphy AM; Poggesi C; Dos Remedios C; Stienen GJ; Ho CY; Michels M; van der Velden J
Circ Res; 2013 May; 112(11):1491-505. PubMed ID: 23508784
[TBL] [Abstract][Full Text] [Related]
14. Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations.
Olivotto I; Girolami F; Sciagrà R; Ackerman MJ; Sotgia B; Bos JM; Nistri S; Sgalambro A; Grifoni C; Torricelli F; Camici PG; Cecchi F
J Am Coll Cardiol; 2011 Aug; 58(8):839-48. PubMed ID: 21835320
[TBL] [Abstract][Full Text] [Related]
15. Cardiomyopathy-related mutation (A30V) in mouse cardiac troponin T divergently alters the magnitude of stretch activation in α- and β-myosin heavy chain fibers.
Mickelson AV; Gollapudi SK; Chandra M
Am J Physiol Heart Circ Physiol; 2017 Jan; 312(1):H141-H149. PubMed ID: 27769999
[TBL] [Abstract][Full Text] [Related]
16. Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy.
Redwood CS; Moolman-Smook JC; Watkins H
Cardiovasc Res; 1999 Oct; 44(1):20-36. PubMed ID: 10615387
[TBL] [Abstract][Full Text] [Related]
17. [Genetics of dilated cardiomyopathy].
Osterziel KJ; Scheffold T; Perrot A; Dietz R;
Z Kardiol; 2001 Jul; 90(7):461-9. PubMed ID: 11515275
[TBL] [Abstract][Full Text] [Related]
18. Novel locus for an inherited cardiomyopathy maps to chromosome 7.
Song L; DePalma SR; Kharlap M; Zenovich AG; Cirino A; Mitchell R; McDonough B; Maron BJ; Seidman CE; Seidman JG; Ho CY
Circulation; 2006 May; 113(18):2186-92. PubMed ID: 16651466
[TBL] [Abstract][Full Text] [Related]
19. Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.
Lakdawala NK; Thune JJ; Colan SD; Cirino AL; Farrohi F; Rivero J; McDonough B; Sparks E; Orav EJ; Seidman JG; Seidman CE; Ho CY
Circ Cardiovasc Genet; 2012 Oct; 5(5):503-10. PubMed ID: 22949430
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation Lys273Glu in the cardiac troponin T gene shows high degree of penetrance and transition from hypertrophic to dilated cardiomyopathy.
Fujino N; Shimizu M; Ino H; Yamaguchi M; Yasuda T; Nagata M; Konno T; Mabuchi H
Am J Cardiol; 2002 Jan; 89(1):29-33. PubMed ID: 11779518
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]